Coux O, Goldberg A L
Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Biol Chem. 1998 Apr 10;273(15):8820-8. doi: 10.1074/jbc.273.15.8820.
Nuclear factor kappaB1 (NF-kappaB) is a heterodimeric complex that regulates transcription of many genes involved in immune and inflammatory responses. Its 50-kDa subunit (p50) is generated by the ubiquitin-proteasome pathway from a 105-kDa precursor (p105). We have reconstituted this proteolytic process in HeLa cell extracts and purified the responsible enzymes. Ubiquitination of p105 requires E1, and either of two types of E2s, E2-25K (for which p105 is the first proven substrate) or a member of the UBCH5 (UBC4) family. It also requires a new E3 of 50 kDa, which we call E3kappaB. This set of enzymes differs from the E2s and E3 reported by others to catalyze p105 ubiquitination in reticulocytes. The ubiquitinating enzymes purified here, together with 26S proteasomes, allowed formation of p50. Thus, the 26S proteasome provides all the proteolytic activities necessary for p105 processing. Interestingly, in the reconstituted system, as observed in cells, the C-terminally truncated form of p105, p97, was processed into p50 more efficiently than normal p105, even when both species were ubiquitinated to a similar extent. Therefore, some additional mechanism involving the C-terminal region of p105 influences the proteolytic processing of the ubiquitinated precursor.
核因子κB1(NF-κB)是一种异二聚体复合物,可调节许多参与免疫和炎症反应的基因的转录。其50 kDa亚基(p50)由泛素-蛋白酶体途径从105 kDa前体(p105)产生。我们在HeLa细胞提取物中重建了这一蛋白水解过程,并纯化了相关酶。p105的泛素化需要E1以及两种E2中的任意一种,即E2-25K(p105是其首个被证实的底物)或UBCH5(UBC4)家族的成员。它还需要一种新的50 kDa的E3,我们称之为E3κB。这组酶与其他人报道的在网织红细胞中催化p105泛素化的E2和E3不同。此处纯化的泛素化酶与26S蛋白酶体一起,促使p50形成。因此,26S蛋白酶体提供了p105加工所需的所有蛋白水解活性。有趣的是,在重建系统中,正如在细胞中观察到的那样,即使两种形式的p105泛素化程度相似,p105的C末端截短形式p97也比正常p105更有效地加工成p50。因此,一些涉及p105 C末端区域的额外机制影响了泛素化前体的蛋白水解加工。